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Our Future Health (OFH)
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Sample details

Our Future Health is a prospective, observational cohort study of the general adult population of the United Kingdom (UK). The programme aims to recruit up to 5 million adults (18 years and older) living in the UK, and so far (December 2025) includes over 1,929,000 participants who have completed baseline health questionnaires. Recruitment began in July 2022, with a focus on enrolling historically underrepresented populations in health research. Participants are routinely followed up through linkage to health and health-related data and recontacted for ongoing biological sampling and questionnaires.

Study design
Cohort - research programme, Cohort - open

Number of participants at first data collection

1,929,752 (participants as of December 2025)

Recruitment is ongoing

Age at first data collection

≥ 18 years (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Adults
Observational cohort
Open cohort
Population-based sample
Prospective cohort
Dataset details
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Countries

England, Northern Ireland, Scotland, United Kingdom of Great Britain and Northern Ireland, Wales

Year of first data collection

2023

Primary Institutions

National Health Service (NHS) (Healthcare/Medical, United Kingdom)

Our Future Health (Third Sector, United Kingdom)

Links

research.ourfuturehealth.org.uk/

healthdatagateway.org/en/data-custodian/86

ourfuturehealth.org.uk/

Profile paper DOI
Not available

Funders

Alnylam Pharmaceuticals, Inc. (Industry, United States of America)

Amgen Inc. (Industry, United States of America)

Asthma + Lung UK (Third Sector, United Kingdom)

AstraZeneca (Industry, United Kingdom)

Biogen Inc. (Industry, United States of America)

Ongoing?
Yes

Data types collected

mentalHealthData
dataLinkage
Quantitative data collection
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Secondary data
  • Self-completed questionnaire – online
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
  • Mortality data
Features

Engagement

  • Patients, service users, lived experience involvement
  • Participant or community advisory groups
  • Community engagement
  • Keywords

    Alcohol use
    Electronic health records
    Environmental exposures
    Family health history
    Genetics
    Lifestyle
    Medical history
    Mental health
    Physical health
    Sociodemographics
    Sub-studies
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